Episodic movement disorders as channelopathies
Identifieur interne : 004A76 ( Main/Exploration ); précédent : 004A75; suivant : 004A77Episodic movement disorders as channelopathies
Auteurs : Kailash P. Bhatia [Royaume-Uni] ; Robert C. Griggs [États-Unis] ; Louis J. Ptá Ek [États-Unis]Source :
- Movement Disorders [ 0885-3185 ] ; 2000-05.
English descriptors
- KwdEn :
- Chorea (genetics), Chorea (physiopathology), Chromosome Mapping, Humans, Ion Channels (genetics), Ion Channels (physiology), Paralyses, Familial Periodic (genetics), Paralyses, Familial Periodic (physiopathology), Spinocerebellar Degenerations (genetics), Spinocerebellar Degenerations (physiopathology).
- MESH :
- chemical , genetics : Ion Channels.
- genetics : Chorea, Paralyses, Familial Periodic, Spinocerebellar Degenerations.
- chemical , physiology : Ion Channels.
- physiopathology : Chorea, Paralyses, Familial Periodic, Spinocerebellar Degenerations.
- Chromosome Mapping, Humans.
Url:
DOI: 10.1002/1531-8257(200005)15:3<429::AID-MDS1001>3.0.CO;2-R
Affiliations:
Links toward previous steps (curation, corpus...)
- to stream Istex, to step Corpus: 003652
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- to stream Istex, to step Checkpoint: 003276
- to stream Main, to step Merge: 007373
- to stream PubMed, to step Corpus: 003F88
- to stream PubMed, to step Curation: 003F88
- to stream PubMed, to step Checkpoint: 003F87
- to stream Ncbi, to step Merge: 000263
- to stream Ncbi, to step Curation: 000263
- to stream Ncbi, to step Checkpoint: 000263
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- to stream Main, to step Curation: 004A76
Le document en format XML
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<term>Ion Channels (physiology)</term>
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